| Title |
Year |
Author |
Number |
| METHOD OF SYNTHESIS OF DERIVATIVES OF (S)-3-AMINO-1-BENZYLPYRROLIDINE, DERIVATIVES OF (S)-AZIRIDINE AS INTERMEDIATE COMPOUNDS FOR THEIR SYNTHESIS AND 1-BENZYL-3-(S)-, 2-(S)-[(TERT-BUTOXYCARBONYLAMINO)PROPIONYLAMINO]-PYRROLIDINE AS AN INTERMEDIATE COMPOUND FOR QUINOLONE-BASE ANTIBACTERIAL AGENTS |
1993 |
- Tung Ven Li[Us]
- Gregori Spens[Us]
- Dzhejms Norton Vempl[Us]
|
RU2101279C1 |
| METHOD OF PREPARING TRANS-6-[SUBSTITUTED PYRROL-1- YL)ALKYL]PYRAN-2-ON DERIVATIVES AND THEIR DIHYDROXY-CONTAINING ACIDS AND SALTS, HYDROXY-, 1,3-DIOXAN- OR PYRROLE-CONTAINING CARBOXYLIC ACIDS AS INTERMEDIATES FOR PREPARING SAID PYRAN-2-ON DERIVATIVES |
1994 |
- Donal'D Ehjdzhin Batler
- Tung Van Li
- Tomas Norman Nanninga
|
RU2138497C1 |
| SULFAMIC ACID ESTERS, PHARMACEUTICAL COMPOSITION FOR CONTROL OF CHOLESTEROL CONCENTRATION, METHOD OF TREATMENT OF PATIENTS WITH HYPERCHOLESTEROLEMIA, METHOD OF TREATMENT OF PATIENTS WITH ATHEROSCLEROSIS |
1994 |
- Khelen Tsenvej Li
- Dzhozef Armend Pikard
- Drago Robert Sliskovits
- Vendell Virendzhe
|
RU2137756C1 |
| AMINOACETIC ACID DERIVATIVES AS RACEMATES OR D-AND L- ENANTIOMERS OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, METHOD OF PREPARING D-AND L-ENANTIOMERS OF AMINOACETIC ACID DERIVATIVES OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, AND AMINOACETIC ACID D-AND L-ENANTIOMERS AS CINCHONIDINE SALTS |
1993 |
- Vladimir Bajlin[Ua]
- Khuaj Gu Chen[Us]
- Om Prakash Gel'[Us]
- Mark Judzhin Marlatt[Us]
- Dzhon Gordon Topliss[Us]
|
RU2111206C1 |
| METHOD OF SYNTHESIS OF 6-CYANOMETHYL-2,2-DIMETHYL-1,3-DIOXANE-4-ACETIC ACID (4R-CIS)-1,1-DIMETHYLETHYL ESTER |
1991 |
- Ehlen Millar[Gb]
- Donel'D Judzhin Batler[Us]
|
RU2067580C1 |
| METHOD OF PRODUCING SUBSTITUTED OCTAHYDRO-1-(W-MERCAPTOALKANOYL)-1H-INDOLE-2-CARBOXYLIC ACID OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF |
0 |
- Milton Luis Khoufl
- Dzhordzh Bobovski
|
SU1246893A3 |
| METHOD OF PRODUCING NAPHTHYRYDINE QUINOLINE- OR BENZOXAZINE CARBOLIC ACIDS OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS OF ACID ADDITION |
0 |
- Taunli P.Kulbertson
- Dzhon M.Domagala
- Tomas F.Mich
- Dzheffri B.Nikols
|
SU1360584A3 |
| DERIVATIVES OF 1,3-SUBSTITUTED CYCLOALKENE AND CYCLOALKANE AS A MIXTURE OF ISOMERS OR INDIVIDUAL ISOMERS OR THEIR HYDRATES, OR SALTS |
1992 |
- Bredlej Villiam Kehpres
- Dennis Majkl Dauning
- Khuan Karlos Dzhejn
- Stifen Dzhozef Dzhonson
- Villiam Dzhon Iii Smit
- Lourens Dejvid Vajs
- Dzhonatan Rajt
- Dejvid Dzhjurgen Vjustro
|
RU2116297C1 |
| DERIVATIVES OF 3-ALKYLHYDROXY-, ARYLHYDROXY- OR ARYLALKYLHYDROXY[B]THIOPHENE-2-CARBOXAMIDE, THEIR PHARMACEUTICALLY ACCEPTABLE SALTS AND PHARMACEUTICAL COMPOSITION SHOWING ACTIVITY INHIBITING ADHESION OF LEUKOCYTES TO VASCULAR ENDOTHELIUM |
1993 |
- Dajen Khehrris Boskelli
- Dehvid Tomas Konnor
- Klifford Din Rajt
|
RU2117665C1 |
| METHODS OF INHIBITION OF TYROSINE KINASE ACTIVITY IN EPIDERMAL GROWTH FACTOR RECEPTORS, BICYCLIC PYRIMIDINE DERIVATIVES, PHARMACEUTICAL COMPOSITION SHOWING ACTIVITY INHIBITING ACTIVITY OF TYROSINE KINASE IN EPIDERMAL GROWTH FACTOR RECEPTORS AND COMPOSITION ELICITING CONTRACEPTIVE EFFECT |
1995 |
- Aleksander Dzhejms Bridzhes
- Uilliam Aleksander Dehnni
- Dehvid Fraj
- Alan Krejker
- Robert Majer
- Gordon Uilliam R'Jukastl
- Ehndrju Mark Tompson
|
RU2174980C2 |
by chlorination of substituted 2,6-dihydroxypyridine derivative of formula II: 
with phosphorus oxychloride in the presence of lithium salt on heated followed by cooling of reaction mixture, dilution with diluent and recovery of chlorination product of formula 
. In order to prepare product (I) wherein R is hydroxyl, said product is reacted with base in the presence of water followed by extraction of the resulting solution with solvent and neutralization with acid. Process proceeds without formation of by-products and with good yield. EFFECT: more efficient preparation method. 10 cl, 3 ex
